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Artigo de periodico
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty (2017)
Dauber, Andrew; Cunha-Silva, Marina; Macedo, Delanie B.; Brito, Vinicius N.; Abreu, Ana Paula; Roberts, Stephanie A.; Montenegro, Luciana R.; Andrew, Melissa; Kirby, Andrew; Weirauch, Matthew T.; Labilloy, Guillaume; Bessa, Danielle S.; Carroll, Rona S.; Jacobs, Dakota C.; Chappell, Patrick E.; Mendonca, Berenice B.; Haig, David; Kaiser, Ursula B.; Latronico, Ana Claudia
Fonte: Journal of clinical endocrinology and metabolism. Unidade: FM
Assuntos: PUBERDADE PRECOCE, REAÇÃO EM CADEIA POR POLIMERASE, HIPOTÁLAMO, MUTAÇÃO GENÉTICA
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ABNT
DAUBER, Andrew et al. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, v. 102, n. 5, p. 1557-1567, 2017Tradução . . Disponível em: https://doi.org/10.1210/jc.2016-3677. Acesso em: 20 jul. 2024.
APA
Dauber, A., Cunha-Silva, M., Macedo, D. B., Brito, V. N., Abreu, A. P., Roberts, S. A., et al. (2017). Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, 102( 5), 1557-1567. doi:10.1210/jc.2016-3677
NLM
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2016-3677
Vancouver
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2016-3677
Artigo de periodico
Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 (2014)
Macedo, Delanie B.; Abreu, Ana Paula; Reis, Ana Claudia S.; Montenegro, Luciana R.; Dauber, Andrew; Beneduzzi, Daiane; Cukier, Priscilla; Silveira, Leticia F. G.; Teles, Milena G.; Carroll, Rona S.; Guerra Junior, Gil; Guaragna Filho, Guilherme; Gucev, Zoran; Arnhold, Ivo J. P.; Castro, Margaret de; Moreira, Ayrton C.; Martinelli Jr., Carlos Eduardo; Hirschhorn, Joel N.; Mendonca, Berenice B.; Brito, Vinicius N.; Antonini, Sonir R.; Kaiser, Ursula B.; Latronico, Ana Claudia
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: FM, FMRP
Assuntos: CRIANÇAS, TÉCNICAS GENÉTICAS, PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA
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ABNT
MACEDO, Delanie B. et al. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. Journal of Clinical Endocrinology and Metabolism, v. 99, n. 6, p. E1097-E1103, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-3126. Acesso em: 20 jul. 2024.
APA
Macedo, D. B., Abreu, A. P., Reis, A. C. S., Montenegro, L. R., Dauber, A., Beneduzzi, D., et al. (2014). Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. Journal of Clinical Endocrinology and Metabolism, 99( 6), E1097-E1103. doi:10.1210/jc.2013-3126
NLM
Macedo DB, Abreu AP, Reis ACS, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LFG, Teles MG, Carroll RS, Guerra Junior G, Guaragna Filho G, Gucev Z, Arnhold IJP, Castro M de, Moreira AC, Martinelli Jr. CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): E1097-E1103.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2013-3126
Vancouver
Macedo DB, Abreu AP, Reis ACS, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LFG, Teles MG, Carroll RS, Guerra Junior G, Guaragna Filho G, Gucev Z, Arnhold IJP, Castro M de, Moreira AC, Martinelli Jr. CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): E1097-E1103.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2013-3126
Artigo de periodico
TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients (2014)
Noel, Sekoni D.; Abreu, Ana Paula; Xu, Shuyun; Muyide, Titilayo; Gianetti, Elena; Tusset, Cintia; Carroll, Jessica; Latronico, Ana Claudia; Seminara, Stephanie B.; Carroll, Rona S.; Kaiser, Ursula B.
Fonte: The FASEB journal. Unidade: FM
Assuntos: SEQUENCIAMENTO GENÉTICO, MUTAÇÃO GENÉTICA (COMPLICAÇÕES), HIPOGONADISMO
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ABNT
NOEL, Sekoni D. et al. TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients. The FASEB journal, v. 28, n. 4, p. 1924-1937, 2014Tradução . . Disponível em: https://doi.org/10.1096/fj.13-240630. Acesso em: 20 jul. 2024.
APA
Noel, S. D., Abreu, A. P., Xu, S., Muyide, T., Gianetti, E., Tusset, C., et al. (2014). TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients. The FASEB journal, 28( 4), 1924-1937. doi:10.1096/fj.13-240630
NLM
Noel SD, Abreu AP, Xu S, Muyide T, Gianetti E, Tusset C, Carroll J, Latronico AC, Seminara SB, Carroll RS, Kaiser UB. TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients [Internet]. The FASEB journal. 2014 ; 28( 4): 1924-1937.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1096/fj.13-240630
Vancouver
Noel SD, Abreu AP, Xu S, Muyide T, Gianetti E, Tusset C, Carroll J, Latronico AC, Seminara SB, Carroll RS, Kaiser UB. TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients [Internet]. The FASEB journal. 2014 ; 28( 4): 1924-1937.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1096/fj.13-240630
Artigo de periodico
Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 (2013)
Abreu, Ana Paula; Dauber, Andrew; Macedo, Delanie B.; Noel, Sekoni D.; Brito, Vinicius N.; Gill, John C.; Cukier, Priscilla; Thompson, Iain R.; Navarro, Victor M.; Gagliardi, Priscila C.; Rodrigues, Tânia; Kochi, Cristiane; Longui, Carlos Alberto; Beckers, Dominique; Zegher, Francis de; Montenegro, Luciana R.; Mendonca, Berenice B.; Carroll, Rona S.; Hirschhorn, Joel N.; Latronico, Ana Claudia; Kaiser, Ursula B.
Fonte: The New England Journal of Medicine. Unidade: FM
Assuntos: PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA, GONADOTROFINAS, REAÇÃO EM CADEIA POR POLIMERASE, BIOLOGIA MOLECULAR, ANÁLISE SEQUENCIAL
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ABNT
ABREU, Ana Paula et al. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3. The New England Journal of Medicine, v. 368, n. 26, p. 2467-2475, 2013Tradução . . Disponível em: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160. Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Dauber, A., Macedo, D. B., Noel, S. D., Brito, V. N., Gill, J. C., et al. (2013). Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3. The New England Journal of Medicine, 368( 26), 2467-2475. doi:10.1056/NEJMoa1302160
NLM
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson IR, Navarro VM, Gagliardi PC, Rodrigues T, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonca BB, Carroll RS, Hirschhorn JN, Latronico AC, Kaiser UB. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 [Internet]. The New England Journal of Medicine. 2013 ; 368( 26): 2467-2475.[citado 2024 jul. 20 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160
Vancouver
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson IR, Navarro VM, Gagliardi PC, Rodrigues T, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonca BB, Carroll RS, Hirschhorn JN, Latronico AC, Kaiser UB. Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3 [Internet]. The New England Journal of Medicine. 2013 ; 368( 26): 2467-2475.[citado 2024 jul. 20 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa1302160
Trabalho de evento-resumo periodico
Loss-of-function mutations in a gene cause central precocius puberty (2013)
Abreu, Ana Paula; Dauber, Andrew; Macedo, Delaine Bulcão; Noel, Sekoni D.; Brito, Vinicius Nahime; Gill, John C.; Cukier, Priscilla; Thompson, Ian; Navarro, Victor M.; Gagliardi, Priscila C.; Rodrigues, Tânia M.; Kochi, Cristiane; Longui, Carlos A.; Beckers, Dominique; Zegher, Francis de; Montenegro, Luciana R.; Mendonça, Berenice Bilharinho de; Carroll, Rona S.; Hirschhorn, Joel N.; Xavier, Ana Claudia Latronico; Kaiser, Ursula B.
Fonte: Hormone Research in Paediatrics. Nome do evento: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Assuntos: PUBERDADE PRECOCE, TRANSTORNOS DO CRESCIMENTO, ENDOCRINOPATIAS
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ABNT
ABREU, Ana Paula et al. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 20 jul. 2024. , 2013
APA
Abreu, A. P., Dauber, A., Macedo, D. B., Noel, S. D., Brito, V. N., Gill, J. C., et al. (2013). Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson I, Navarro VM, Gagliardi PC, Rodrigues TM, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonça BB de, Carroll RS, Hirschhorn JN, Xavier ACL, Kaiser UB. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. 2013 ; 80 35.[citado 2024 jul. 20 ]
Vancouver
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson I, Navarro VM, Gagliardi PC, Rodrigues TM, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonça BB de, Carroll RS, Hirschhorn JN, Xavier ACL, Kaiser UB. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. 2013 ; 80 35.[citado 2024 jul. 20 ]
Artigo de periodico
A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations (2012)
Abreu, Ana Paula; Xu, Shuvun; Noel, Sekomi D.; Carroll, Rona S.; Kaiser, Ursula B.; Latronico, Ana C.
Fonte: Endocrine Reviews. Nome do evento: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo. Unidade: FM
Assuntos: PUBERDADE PRECOSE, WESTERN BLOTTING, HIPOGONADISMO, MUTAÇÃO GENÉTICA, RESUMOS (EVENTOS)
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ABNT
ABREU, Ana Paula et al. A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-620. Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Xu, S., Noel, S. D., Carroll, R. S., Kaiser, U. B., & Latronico, A. C. (2012). A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-620
NLM
Abreu AP, Xu S, Noel SD, Carroll RS, Kaiser UB, Latronico AC. A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 jul. 20 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-620
Vancouver
Abreu AP, Xu S, Noel SD, Carroll RS, Kaiser UB, Latronico AC. A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 jul. 20 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-620
Artigo de periodico
Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function (2012)
Abreu, Ana Paula; Noel, Sekoni D.; Xu, Shuyun; Carroll, Rona S.; Latronico, Ana Claudia; Kaiser, Ursula B.
Fonte: Molecular Endocrinology. Unidade: FM
Assuntos: BIOLOGIA MOLECULAR (PROCESSOS), CÉLULAS DENDRÍTICAS (ANÁLISE), HIPOGONADISMO (GENÉTICA), MUTAÇÃO GENÉTICA, VETORES
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ABNT
ABREU, Ana Paula et al. Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function. Molecular Endocrinology, v. 26, n. 8, p. 1417-1427, 2012Tradução . . Disponível em: http://intl-mend.endojournals.org/content/26/8/1417.full.pdf+html. Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Noel, S. D., Xu, S., Carroll, R. S., Latronico, A. C., & Kaiser, U. B. (2012). Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function. Molecular Endocrinology, 26( 8), 1417-1427. doi:10.1210/me.2012-1102
NLM
Abreu AP, Noel SD, Xu S, Carroll RS, Latronico AC, Kaiser UB. Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function [Internet]. Molecular Endocrinology. 2012 ; 26( 8): 1417-1427.[citado 2024 jul. 20 ] Available from: http://intl-mend.endojournals.org/content/26/8/1417.full.pdf+html
Vancouver
Abreu AP, Noel SD, Xu S, Carroll RS, Latronico AC, Kaiser UB. Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function [Internet]. Molecular Endocrinology. 2012 ; 26( 8): 1417-1427.[citado 2024 jul. 20 ] Available from: http://intl-mend.endojournals.org/content/26/8/1417.full.pdf+html

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